Spring + Summer 2027 Co-Op - Manufacturing Science & Technology

Alcon • Houston, TX

7d • Onsite

About The Position

The Alcon team is looking for talented and motivated CO-OP to join us on-site in Spring 2027 at the Houston, TX location to support risk management documentation remediation activities across manufacturing processes and product lines. Working under the guidance of MS&T, Quality, and Operations stakeholders, this role will assist in reviewing, organizing, and updating documentation to improve alignment between risk assessments, failure analyses, and process controls. This position is well suited for a student who is highly organized, detail-oriented, and interested in applying engineering skills in a regulated environment. This role will partner cross-functionally with Engineering, Quality, and Operations teams in support of compliance with internal procedures and applicable regulatory expectations. Alcon interns will have the opportunity to not only gain industry experience and network with other Alcon professionals. They will also have the chance to make a real-world impact by working on meaningful projects that will help patients and customers see brilliantly. Alcon also offer CO-OP individuals personal and professional development, high visibility and coaching and mentoring opportunities.

Requirements

• Must be enrolled in an accredited university or college for at least one semester prior to the internship, and at least one additional semester following your internship
• Must be pursuing a Bachelor's or Master's degree
• Academic performance: Minimum cumulative GPA 2.8/4.0
• Demonstrated leadership skills (i.e. extracurricular activities or projects)
• Must be authorized to work in the US on a permanent basis. Students on an F1 visa with CPT work authorization may be accommodated
• Ability to commit to a co-op for the Spring and Summer semesters, full time (40 hrs/week) project

Nice To Haves

• Exposure to risk management principles and engineering risk documentation.
• Familiarity with FMEA concepts and structured problem-solving or root cause analysis methodologies.
• Experience working with Excel and other Microsoft Office tools, including PowerPoint, Outlook, Teams, SharePoint, and related project-tracking tools.
• Ability to work collaboratively with cross-functional teams and independently on assigned tasks.
• Interest in medical device, pharmaceutical, or other regulated manufacturing environments.

Responsibilities

• Support assigned risk management remediation workstreams by organizing action items, tracking milestones, and maintaining project documentation.
• Assist in reviewing risk management documents, failure analyses, and related control documentation for consistency, completeness, and traceability.
• Update assigned documentation based on approved inputs, stakeholder feedback, and established templates.
• Help prepare and maintain trackers, meeting notes, status summaries, and documentation packages for assigned scope.
• Support mapping of manufacturing process flows and documentation linkages to aid identification of potential gaps in collaboration with subject matter experts.
• Coordinate cross-functional meetings, capture discussion outcomes, and communicate follow-up actions clearly and professionally.
• Organize large volumes of technical information and documentation across multiple parallel workstreams.
• Escalate issues, missing inputs, or timeline risks to the project lead or functional stakeholder, as appropriate.
• Contribute to clear, audit-ready documentation updates that support ongoing risk management remediation efforts.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: No Education Listed